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| Ataxia and cerebellar anomalies - narrow panel v0.5 | TINF2 |
Ellen McDonagh gene: TINF2 was added gene: TINF2 was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: TINF2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TINF2 were set to 18979121; 18252230 Phenotypes for gene: TINF2 were set to Dyskeratosis congenita, autosomal dominant 3 613990 |
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